Canonical Allele Identifier: CA1180934333

Linked Data

dbSNP Id: rs1687191416
gnomAD v4: 1-92837934-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837934A>G , CM000663.2:g.92837934A>G GRCh38
NC_000001.10:g.93303491A>G , CM000663.1:g.93303491A>G GRCh37
NC_000001.9:g.93076079A>G NCBI36
NG_011779.1:g.10898A>G
NG_033051.1:g.128589T>C
NG_011779.2:g.10949A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+301A>G (RPL5) MANE Select ENSP00000359345.2:n.705+301A>G
ENST00000645119.1:c.325-2617A>G (RPL5) ENSP00000493811.1:n.325-2617A>G
ENST00000645300.1:c.555+301A>G (RPL5) ENSP00000495589.1:n.555+301A>G
ENST00000370321.7:c.705+301A>G (RPL5) ENSP00000359345.2:n.705+301A>G
ENST00000497519.1:n.1024+301A>G (RPL5)
ENST00000615519.4:c.475-4900T>C (DIPK1A) ENSP00000483279.1:n.475-4900T>C
NM_000969.3:c.705+301A>G (RPL5) NP_000960.2:n.705+301A>G
NM_001252273.1:c.475-4900T>C (DIPK1A) NP_001239202.1:n.475-4900T>C
NM_000969.5:c.705+301A>G (RPL5) MANE Select NP_000960.2:n.705+301A>G
NR_146333.1:n.764+301A>G (RPL5)
NM_001252273.2:c.475-4900T>C (DIPK1A) NP_001239202.1:n.475-4900T>C